Results 71 to 80 of about 435 (109)

Hemocromatose hereditária: relato de caso clínico e revisão da literatura

, 2009
The work tells the case of a carrying patient of Hereditary Hemochromatosis (HH) that it is if benefiting of the precocious diagnosis and the accomplishment of weekly bleedings associated to the Chelation therapy, what very reduced the impregnation of ...
ARRUDA, Victor Moreira, SARAIVA, Maiana Moura   +1 more
core   +1 more source

REVISÃO SISTEMÁTICA SOBRE A PREVALÊNCIA DE HEMOCROMATOSE HEREDITÁRIA NO BRASIL E SUA INCLUSÃO NA DOAÇÃO DE SANGUE

Hematology, Transfusion and Cell Therapy
Objetivo: Sintetizar as evidências sobre a prevalência de Hemocromatose Hereditária (HH) na população brasileira e discutir a inclusão desses doadores na política nacional de doação de sangue, comparando os resultados com a literatura mundial.
LAR Ono, SCO Gilli
doaj   +1 more source

Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotype. [PDF]

Hepatol Int, 2018
Adams P, Altes A, Brissot P, Butzeck B, Cabantchik I, Cançado R, Distante S, Evans P, Evans R, Ganz T, Girelli D, Hultcrantz R, McLaren G, Marris B, Milman N, Nemeth E, Nielsen P, Pineau B, Piperno A, Porto G, Prince D, Ryan J, Sanchez M, Santos P, Swinkels D, Teixeira E, Toska K, Vanclooster A, White D, Contributors and Hemochromatosis International Taskforce.   +29 more
europepmc   +1 more source

Brazilian Nutritional Consensus in Hematopoietic Stem Cell Transplantation: Graft- versus -host disease. [PDF]

Einstein (Sao Paulo), 2020
Pereira AZ, Vigorito AC, Almeida AM, Candolo AA, Silva ACL, Brandão-Anjos AEP, Sá BL, Souza CLS, Castro Junior CG, Oliveira JSR, Barban JB, Mancilha EMB, Todaro J, Lopes LP, Macedo MCMA, Rodrigues M, Ribeiro PC, Silva RLD, Roberto TS, Rodrigues TCR, Colturato VAR, Paton EJA, Barros GMN, Almeida RDS, Moreira MCR, Flowers ME.   +25 more
europepmc   +1 more source

Padronização de técnica de PCR em tempo real para detecção simultânea das mutações H63D e S65C no gene HFE da hemocromatose [PDF]

, 2012
Hemochromatosis is the most common genetic disorder in Caucasians. Its geographic distribution is worldwide, but it is seen most commonly in some populations in which it occurs with a prevalence of approximately 1 per 220-250 individuals.
FREDERICO SCOTT VARELLA MALTA
core  

Hemocromatose hereditária: da genética ao manejo clínico

A hemocromatose é um distúrbio hereditário recessivo, caracterizado pela sobrecarga de ferro em diferentes órgãos e tecidos, especialmente fígado, pâncreas, coração, pele e articulações.
Rodrigues, Laura Oliveira de Paula, Luiz, Deise Girardi, Machado, Indiara Pacheco, Kowalski, Thayne Woycinck, Oliveira, Maria Eduarda Moreira de, Machado, Amanda Köhn   +5 more
core  

Mutações genéticas, métodos diagnósticos e terapêuticas relacionadas à hemocromatose hereditária

, 2014
Hereditary haemochromatosis is a genetic disease related to various iron metabolism disorders and a major cause of iron overload. The technical and scientiic advances obtained over the last decades, particularly with the development of molecular biology,
Aguiar, Karina Marini, Xavier, Mauro Aparecido de Souza, Colares, Thalles Danylo Souza, Xavier, Alessandra Rejane Ericsson de Oliveira   +3 more
core  

Hemocromatose hereditária: resposta celular ao stress oxidativo [PDF]

, 2013
Mestrado em Bioquímica - Bioquímica ClínicaIron is a key element for basic cellular functions. If iron homeostasis is not maintained it may lead to iron overload.
Andrade, Lara Filipe Rocha
core  

Ferritin light chain gene mutations in two Brazilian families with hereditary hyperferritinemia-cataract syndrome. [PDF]

Einstein (Sao Paulo), 2017
Petroni RC, Rosa SEAD, Carvalho FP, Santana RAF, Hyppolito JE, Nascimento CMDB, Hamerschlak N, Campregher PV.   +7 more
europepmc   +1 more source

Brazilian Cardiology Society Statement for Management of Pregnancy and Family Planning in Women with Heart Disease - 2020. [PDF]

Arq Bras Cardiol, 2020
Avila WS, Alexandre ERG, Castro ML, Lucena AJG, Marques-Santos C, Freire CMV, Rossi EG, Campanharo FF, Rivera IR, Costa MENC, Rivera MAM, Carvalho RCM, Abzaid A, Moron AF, Ramos AIO, Albuquerque CJDM, Feio CMA, Born D, Silva FBD, Nani FS, Tarasoutchi F, Costa Junior JR, Melo Filho JX, Katz L, Almeida MCC, Grinberg M, Amorim MMR, Melo NR, Medeiros OO, Pomerantzeff PMA, Braga SLN, Cristino SC, Martinez TLDR, Leal TCAT.   +33 more
europepmc   +1 more source